carbazole

BrCCCCCCCCCCn1c2ccccc2c2ccccc21
Reaction #11838
N-(10-bromodecyl)-carbazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc2c(c1)c1ccccc1n2-c1ccc(-c2ccc(-n3c4ccccc4c4ccccc43)cc2)cc1
Reaction #44311
4,4′-bis(carbazol-9-yl)biphenyl
収率 75527.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCn1c2ccccc2c2ccccc21
Reaction #64660
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=O)c1ccc(-n2c3ccccc3c3ccccc32)cc1
Reaction #66035
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1ccc2[nH]c3ccccc3c2c1
Reaction #70058
white powdered solid
収率 76989.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1ccc(-n2c3ccccc3c3ccccc32)cc1
Reaction #70062
9-(4-bromophenyl)-9H-carbazole
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)n1c2ccccc2c2ccccc21
Reaction #77734
9-acetyl-carbazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
c1ccc(-c2c3ccccc3c(-c3cccc(-n4c5ccccc5c5ccccc54)c3)c3ccccc23)cc1
Reaction #167473
light-yellow solid
収率 73.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc(-c2c3ccccc3c(-c3ccccc3)c3cc(-n4c5ccccc5c5ccccc54)ccc23)cc1
Reaction #167474
9-(9,10-diphenyl-2-anthryl)-9H-carbazole
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
c1ccc(Cn2c3ccccc3c3ccccc32)cc1
Reaction #178598
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1ccc2[nH]c3ccccc3c2c1
Reaction #180064
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCn1c2ccccc2c2ccccc21
Reaction #186589
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(Cn2c3ccccc3c3ccccc32)cc1
Reaction #201254
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
BrCCCn1c2ccccc2c2ccccc21
Reaction #209032
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(-c2c3ccccc3c(-c3ccccc3)c3cc(-n4c5ccccc5c5ccccc54)ccc23)cc1
Reaction #225232
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(Cn2c3ccccc3c3ccccc32)cc1
Reaction #230138
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(-n2c3ccccc3c3ccccc32)cc1
Reaction #232982
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C1=C(n2c3ccccc3c3ccccc32)Cc2ccccc21
Reaction #255346
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(-n2c3ccccc3c3ccccc32)cc1
Reaction #257964
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Brc1ccc(-n2c3ccccc3c3ccccc32)cc1
Reaction #272158
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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